참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | tert-Butyl methyl ether | HCID 15413 | — |
| 반응물 | 2-Hydroxy-3′,4′-dihydroxyacetophenone | HCID 22134444 | — |
| 생성물 | 1,2-Benzenediol, 4-(3-hydroxypropyl)- | HCID 11217464 | — |
반응 단계
A special house made pressure reactor, a 50 ml 10 bar glass reactor with steel mantle and a magnetic stirring bar, was charged with catalyst, 4-hydroxyacetyl-catechol (produced according to Example 2) and t-butyl methyl ether. The reactor was evacuated and filled with hydrogen. Hydrogenation was started by stirring at 5 bar hydrogen pressure while heating to 40° C. By the end of the reaction the hydrogen was replaced by air, the slurry was filtered, the catalyst was washed with ethyl acetate. After evaporation of the solvents and drying at 1 mbar the product was analyzed quantitatively. The details of some reactions and the results are shown in Table 1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08017815B2 |
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| 출처 데이터셋 | uspto-grants-2011_09 |
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| ORD ID | ord-3c54dba0bde4486c8305ae18deb44e6c |
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| 출처 메모 | uspto-grants-2011_09 |
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